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BS EN 61326-2-6:2013

Superseded
Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by
superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

Electrical equipment for measurement, control and laboratory use. EMC requirements Particular requirements. In vitro diagnostic (IVD) medical equipment
Available format(s)

Hardcopy , PDF

Superseded date

08-06-2021

Language(s)

English

Published date

31-07-2013

1 Scope
2 Normative references
3 Terms and definitions
4 General
5 EMC test plan
6 Immunity requirements
7 Emission requirements
8 Test results and test report
9 Instructions for use
Annex A (normative) - Immunity test requirements
        for portable test and measurement equipment
        powered by battery or from the circuit being
        measured
Bibliography
Annex ZA (normative) - Normative references to
         international publications with their
         corresponding European publications
Annex ZZ (informative) - Coverage of Essential
         Requirements of EU Directives

Describes minimum requirements for immunity and emissions regarding electromagnetic compatibility for in vitro diagnostic medical equipment, taking into account the particularities and specific aspects of this electrical equipment and their electromagnetic environment.

IEC 61326-2-6:2012 specifies minimum requirements for immunity and emissions regarding electromagnetic compatibility for in vitro diagnostic medical equipment, taking into account the particularities and specific aspects of this electrical equipment and their electromagnetic environment. This second edition cancels and replaces the first edition published in 2005 and constitutes a technical revision. It includes the following significant technical change: update of the document with respect to IEC 61326-1:2012.

This publication is to be read in conjunction with IEC 61326-1:2012.

Committee
GEL/65/1
DevelopmentNote
To be read in conjunction with BS EN 61326-1. Supersedes 04/30116660 DC. (06/2006) Together with BS EN 61326-1, BS EN 61326-2-1, BS EN 61326-2-2, BS EN 61326-2-3, BS EN 61326-2-4, BS EN 61326-2-5, BS EN 61326-3-1 and BS EN 61326-3-2, supersedes BS EN 61326. (01/2009) Supersedes 10/30216029 DC. (07/2013)
DocumentType
Standard
Pages
16
PublisherName
British Standards Institution
Status
Superseded
SupersededBy
Supersedes

Standards Relationship
DIN EN 61326-2-6 : 2013 Identical
IEC 61326-2-6:2012 Identical
NF EN 61326-2-6 : 2013 Identical
UNE-EN 61326-2-6:2006 Identical
EN 61326-2-6:2013 Identical
NBN EN 61326-2-6 : 2013 Identical
SN EN 61326-2-6 : 2006 Identical

ISO 18113-1:2009 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements
IEEE/ANSI C63.18-2014 REDLINE American National Standard Recommended Practice for an On-Site, Ad Hoc Test Method for Estimating Electromagnetic Immunity of Medical Devices to Radiated Radio-Frequency (RF) Emissions from RF Transmitters
EN 61326-1:2013 Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 1: General requirements
AAMI TIR18:2010 GUIDANCE ON ELECTROMAGNETIC COMPATIBILITY OF MEDICAL DEVICES IN HEALTHCARE FACILITIES
EN ISO 14971:2012 Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)
ISO 14971:2007 Medical devices Application of risk management to medical devices

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